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Global Clinical Project Jobs (NOW HIRING)

Parexel

Global Clinical Lead / Global Lead

Raleigh, NC · On-site

You will serve as the primary clinical liaison to project leadership and sponsor teams coordinating ... Lead global clinical operations strategy and execution for assigned clinical trials. * Drive study ...

Parexel

Global Clinical Lead / Global Lead

Raleigh, NC · On-site

You will serve as the primary clinical liaison to project leadership and sponsor teams coordinating ... Lead global clinical operations strategy and execution for assigned clinical trials. * Drive study ...

ICON

Senior Clinical Project Manager

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Project Manager - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Icon plc

Senior Clinical Project Manager

Blue Bell, PA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Senior Clinical Project Manager - Remote, US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Telix Pharmaceuticals (AMER)

OR · On-site

The SCPM is responsible for the successful execution of national and global clinical trials (early ... Ensuring effective project plans are in place and operational for each trial within trial ...

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Global Clinical Project information

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How much do global clinical project jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for global clinical project in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a global clinical project manager, and why are they important?

To thrive as a Global Clinical Project Manager, you need expertise in clinical research, project management, and regulatory compliance, usually supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and project management certifications like PMP or PRINCE2 is highly valuable. Exceptional leadership, cross-cultural communication, and problem-solving skills help drive complex, multinational teams and projects forward. These skills ensure efficient, compliant execution of global clinical trials, ultimately supporting successful drug development and patient safety.

What is a global clinical project manager?

A Global Clinical Project Manager is a professional responsible for overseeing and coordinating clinical trials that are conducted in multiple countries. They ensure that the trials adhere to regulatory guidelines, meet timelines and budgets, and maintain high standards of quality and safety. Their role involves managing cross-functional teams, collaborating with stakeholders worldwide, and addressing challenges that arise from conducting trials across diverse regulatory and cultural environments.

What is the difference between Global Clinical Project vs Clinical Trial Coordinator?

AspectGlobal Clinical ProjectClinical Trial Coordinator
ResponsibilitiesOversees multiple clinical trials across regions, manages project timelines, budgets, and cross-functional teamsAssists in trial setup, coordinates site activities, and ensures protocol adherence at specific sites
Required CredentialsTypically requires a degree in life sciences, clinical research experience, and project management skillsUsually requires a degree in health sciences or related field, with experience in clinical trial operations
Work EnvironmentGlobal offices, multinational teams, and cross-regional sitesClinical sites, hospitals, or research centers

The Global Clinical Project role involves managing large-scale, multi-region clinical trials, focusing on strategic oversight and coordination. In contrast, the Clinical Trial Coordinator handles day-to-day site activities and trial logistics. Both roles require clinical research knowledge, but the Global Clinical Project position demands broader project management skills and international experience.

How does a global clinical project manager typically collaborate with cross-functional and international teams during a study?

A Global Clinical Project Manager regularly coordinates with cross-functional teams—including regulatory affairs, data management, biostatistics, and clinical operations—across multiple countries. They facilitate clear communication, oversee timelines, and resolve logistical challenges that arise from working with diverse teams and time zones. Effective collaboration involves regular meetings, shared digital platforms, and adapting to different cultural expectations, all to ensure the study progresses smoothly and complies with global regulations. Building strong relationships and fostering open communication are essential for project success.
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What job categories do people searching Global Clinical Project jobs look for?

The top searched job categories for Global Clinical Project jobs are:

Infographic showing various Global Clinical Project job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Global Clinical Project Leader

Celldex Therapeutics

New Haven, CT • On-site

$176K - $229K/yr

Other

Medical, Retirement, PTO

Re-posted 24 days ago

Job description

About Celldex
Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a culture where innovative and talented people thrive-focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. In our highly entrepreneurial environment, employees are empowered and the opportunity for professional development occurs every day.
Overview
The Global Clinical Project Leader will provide overarching management of clinical trial execution for the assigned clinical development program. The incumbent will be responsible for developing the tactical portion of the operational component of the clinical development plan; in consultation with key stakeholders, including high level resourcing (timelines, budget, and resources), development of clinical project standards, tools, metrics, and assessing the impact of any proposed changes to the program. The incumbent will be responsible for employing risk-based management strategies, implementing solutions, and providing accurate and timely information on the program and fostering continuous improvement in clinical development.
Responsibilities
  • Develop and deliver on operational component of the clinical development plan in consultation with key stakeholders, including:
    • High level resource planning
    • High level budget oversight
    • Clinical drug supply requirements
    • Development of clinical program standards; and
    • Assessing impact of any proposed changes to the program
  • Oversee matrix relationship with assigned Clinical trial Managers, Data Managers, and other members of the Clinical Project Team; ensure consistent execution across the program, deliver a development package of adequate quality for product registration.
  • Represent development operations in cross-functional strategy and program team meetings.
  • Detect possible operational issues/risks in the clinical development programs and assist CTMs in developing mitigation plans. Propose and implement solutions to issues/risks.
  • Provide accurate and timely information on the program.
  • Facilitate continuous improvement in clinical development.
  • Stay abreast of clinical operations developments, methods, and technologies related to the biotechnology/pharmaceutical industry. Make strategic and tactical recommendations to provide and ensure competitive advantage to the company.
  • Other job-related duties as assigned.

Qualifications
  • Completed BS degree or equivalent, with a minimum of 8 years pharmaceutical or biotechnology industry experience; or completed MS degree or equivalent with a minimum of 6 years pharmaceutical or biotechnology industry experience, at least 2 of which must have been at the Senior Clinical Trial Manager or equivalent position.
  • Planning and managing complex and/or strategic priority clinical programs.
  • Dermatology and Allergy experience preferred.
  • Technology aptitude (project management, eTMF, etc.)
  • Experience with data review, analysis, and interpretation of data.
  • In-depth knowledge of the drug development and commercialization process (from protocol writing to medical results reporting and submissions.)
  • In-depth knowledge of Good Clinical Practices (GCP), federal regulations and international regulations.
  • Proven people management expertise.
  • Ability to effectively influence without hierarchical authority.
  • Flexibility and drive for results - willingness to embrace change and be able to work in a changing environment while being driven to achieve goals.
  • Strong communication skills to ensure that project plans and status are transparent, and that risks, issues and results are clear to all parties involved.
  • Strength and depth of skills in gathering information for decision-making; negotiation; and communicating decisions and actions.
  • Able to work both independently and collaboratively across cultures and geographies.
  • Strong computer skills including knowledge of Microsoft Excel, Word, and Outlook.
  • Ability to work within established timelines, in a fast-paced environment.
  • Excellent organizational and priority management skills.
  • Good interpersonal skills and ability to deal with people at all levels with sensitivity and tact.

Compensation
The expected base salary range for this position is $176,659 to $229,427
We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.
Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.
Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.

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